Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 5.9E-02 0 0
CUI: C0014574
Disease: Epiphysitis
Epiphysitis 		1 0 1 5.9E-02 0 0
CUI: C0016479
Disease: Food Poisoning
Food Poisoning 		1 0 1 5.9E-02 0 0
CUI: C0085388
Disease: Intracranial Tuberculoma
Intracranial Tuberculoma 		1 0 1 5.9E-02 0 0
CUI: C0154834
Disease: Retinal Microaneurysm
Retinal Microaneurysm 		1 0 1 5.9E-02 0 0
CUI: C0154884
Disease: Acute posterior multifocal placoid pigment epitheliopathy
Acute posterior multifocal placoid pigment epitheliopathy 		1 0 1 5.9E-02 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 5.9E-02 0 0
CUI: C0202123
Disease: Luteinizing hormone measurement
Luteinizing hormone measurement 		1 0 1 5.9E-02 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 5.9E-02 0 0
CUI: C0238309
Disease: Ischemic peripheral neuropathy
Ischemic peripheral neuropathy 		1 0 1 5.9E-02 0 0
CUI: C0238814
Disease: brain hemangioma
brain hemangioma 		1 0 1 5.9E-02 0 0
CUI: C0241831
Disease: Cerebral salt-wasting syndrome
Cerebral salt-wasting syndrome 		1 0 1 5.9E-02 0 0
CUI: C0265831
Disease: Congenital absence of pulmonic valve
Congenital absence of pulmonic valve 		1 0 1 5.9E-02 0 0
CUI: C0266782
Disease: Abnormal yolk sac
Abnormal yolk sac 		1 0 1 5.9E-02 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 5.9E-02 0 0
CUI: C0271086
Disease: Toxic maculopathy
Toxic maculopathy 		1 0 1 5.9E-02 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 5.9E-02 0 0
CUI: C0275909
Disease: Tuberculosis of brain
Tuberculosis of brain 		1 0 1 5.9E-02 0 0
CUI: C0339825
Disease: Nasal vestibulitis
Nasal vestibulitis 		1 0 1 5.9E-02 0 0
CUI: C0340561
Disease: Arterial ischemia
Arterial ischemia 		1 0 1 5.9E-02 0 0
CUI: C0340648
Disease: dissection of coronary artery
dissection of coronary artery 		1 0 1 5.9E-02 0 0
CUI: C0341037
Disease: Lateral developmental cyst of jaw
Lateral developmental cyst of jaw 		1 0 1 5.9E-02 0 0
CUI: C0343381
Disease: Verotoxigenic Escherichia coli gastrointestinal tract infection
Verotoxigenic Escherichia coli gastrointestinal tract infection 		1 0 1 5.9E-02 0 0
CUI: C0399553
Disease: Mandibular deviation
Mandibular deviation 		1 0 1 5.9E-02 0 0
CUI: C0403411
Disease: Endocapillary glomerulonephritis
Endocapillary glomerulonephritis 		1 0 1 5.9E-02 0 0